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Statistical analysis plan for the replacing protein via enteral nutrition in a stepwise approach in critically ill patients (REPLENISH) randomized clinical trial

Authors :
Yaseen M Arabi
Hasan M. Al-Dorzi
Omar Aldibaasi
Musharaf Sadat
Jesna Jose
Dina Muharib
Haifa Algethamy
Abdulrahman A. Al-Fares
Fahad Al-Hameed
Ahmed Mady
Ayman Kharaba
Ali Al Bshabshe
Khalid Maghrabi
Khalid AlGhamdi
Ghulam Rasool
Adnan AlGhamdi
Ghaleb. A Almekhlafi
Jamal Chalabi
Haifaa Ibrahim AlHumedi
Maram Hasan Sakkijha
Norah Khalid Alamrey
Amjad Sami Alaskar
Rabeah Hamad Alhutail
Kaouthar Sifaoui
Rakan Alqahtani
Ahmad S. Qureshi
Mohammed Moneer Hejazi
Hatim Arishi
Samah AlQahtani
Amro Mohamed Ghazi
Saleh T. Baaziz
Abeer Othman Azhar
Sara Fahad Alabbas
Mohammed AlAqeely
Ohoud AlOrabi
Aliaa Al-Mutawa
Maha AlOtaibi
Madiha Fawazy Elghannam
Mohammed Almaani
Sarah Fadel Buabbas
Wadiah Alawi M. Alfilfil
Mohammed S. Alshahrani
Joel Starkopf
Jean-Charles Preiser
Anders Perner
Jumana Hani AlMubarak
Wafa Mansoor Hazem
Talal Albrahim
Abdulaziz Al-Dawood
and the Saudi Critical Care Trials Group
Source :
Trials, Vol 25, Iss 1, Pp 1-10 (2024)
Publication Year :
2024
Publisher :
BMC, 2024.

Abstract

Abstract Background The optimal amount and timing of protein intake in critically ill patients are unknown. REPLENISH (Replacing Protein via Enteral Nutrition in a Stepwise Approach in Critically Ill Patients) trial evaluates whether supplemental enteral protein added to standard enteral nutrition to achieve a high amount of enteral protein given from ICU day five until ICU discharge or ICU day 90 as compared to no supplemental enteral protein to achieve a moderate amount of enteral protein would reduce all-cause 90-day mortality in adult critically ill mechanically ventilated patients. Methods In this multicenter randomized trial, critically ill patients will be randomized to receive supplemental enteral protein (1.2 g/kg/day) added to standard enteral nutrition to achieve a high amount of enteral protein (range of 2–2.4 g/kg/day) or no supplemental enteral protein to achieve a moderate amount of enteral protein (0.8–1.2 g/kg/day). The primary outcome is 90-day all-cause mortality; other outcomes include functional and health-related quality-of-life assessments at 90 days. The study sample size of 2502 patients will have 80% power to detect a 5% absolute risk reduction in 90-day mortality from 30 to 25%. Consistent with international guidelines, this statistical analysis plan specifies the methods for evaluating primary and secondary outcomes and subgroups. Applying this statistical analysis plan to the REPLENISH trial will facilitate unbiased analyses of clinical data. Conclusion Ethics approval was obtained from the institutional review board, Ministry of National Guard Health Affairs, Riyadh, Saudi Arabia (RC19/414/R). Approvals were also obtained from the institutional review boards of each participating institution. Our findings will be disseminated in an international peer-reviewed journal and presented at relevant conferences and meetings. Trial registration ClinicalTrials.gov, NCT04475666 . Registered on July 17, 2020.

Details

Language :
English
ISSN :
17456215
Volume :
25
Issue :
1
Database :
Directory of Open Access Journals
Journal :
Trials
Publication Type :
Academic Journal
Accession number :
edsdoj.3fcfbdc04e4d4a87abd08e5f3ab344c0
Document Type :
article
Full Text :
https://doi.org/10.1186/s13063-024-08105-w